CYYR1

Cysteine and tyrosine rich 1 Q96J86 CYYR1_HUMAN
Protein Coding Chr 21 21q21.3 Swiss-Prot reviewed Entrez 116159
Mutations
274
CL 38 · Tissue 231
Samples
165
CL 25 · Tissue 137
Peptides
126
unique mutant peptides
Transcripts
3
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

TotalCell lineTissue
Mutations27438231
Samples16525137
Peptides12618110

Function

CYYR1 · Cysteine and tyrosine rich 1

Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

3 transcripts · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000299340 Q96J86 162 114
ENST00000400043 Q96J86-3 104 75
ENST00000652641 Q96J86-2 8 8

Gene Properties

Type
Protein Coding
Chromosome
21
Cytoband
21q21.3
Entrez ID
Aliases
C21orf95

Recurrent Mutations

All 114 amino-acid changes on canonical ENST00000299340 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation frequency across cancer types

% of samples with a missense/complex mutation in CYYR1 · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in CYYR1 – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Glioblastoma
2/98 2%
0/0 0%
Melanoma
0/210 0%
33/1899 2%
Non-Small Cell Lung Carcinoma
8/304 3%
18/1390 1%
Endometrial Carcinoma
0/42 0%
5/612 1%
Gastric Carcinoma
0/74 0%
14/1809 1%
Small Cell Lung Carcinoma
1/9 11%
4/752 1%
Colorectal Carcinoma
2/143 1%
20/3239 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Hepatocellular Carcinoma
2/46 4%
8/2210 0%
Other Sarcomas
3/69 4%
0/699 0%
Glioma
0/52 0%
7/2127 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Pancreatic Carcinoma
0/89 0%
4/1611 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
6/2534 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Kidney Carcinoma
4/85 5%
0/1862 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Other Solid Cancers
1/94 1%
2/1515 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Prostate Carcinoma
0/13 0%
2/2105 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
B-Lymphoblastic Leukemia
1/55 2%
1/2640 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where CYYR1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CYYR1 were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 54 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 274 mutations in CYYR1

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide